Taiy Chemical
METHYL-D3-AMINE HYDROCHLORIDE
Product Name Methyl-d3-amine hydrochloride
Synonyms:5143 (~2~H_3_)methanamine hydrochloride
CAS RN. 7436-22-8
EINECS 231-089-6
Molecular Weight 70.5365
Molecular Formula CH3D3ClN
Melting Point(℃) 229-232℃
Hazard Symbols Xi Details
Xi
Risk Codes  R36/37/38;    Details
 R36/37/38;     Details
Safety Description  S24/25;Details
 S24/25; Details
FAQ
What is Methyl-D3-Amine Hydrochloride and how does it work?

Methyl-D3-Amine Hydrochloride, often referred to as MDAH, is a chemical compound that is commonly used as a reagent in organic synthesis. It is a derivative of amine and belongs to the class of methylamines. MDAH is known for its ability to act as a powerful nucleophile, making it a valuable tool in various chemical reactions. When MDAH reacts with certain compounds, it can undergo substitution reactions, leading to the formation of new chemical bonds.

What are the main applications of Methyl-D3-Amine Hydrochloride?

MDAH has a wide range of applications in the field of organic chemistry. It is commonly used as a reagent in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. MDAH can be used in reactions such as reductive amination, reductive alkylation, and reductive coupling. It is also used in the production of dyes, polymers, and other industrial chemicals. Additionally, MDAH is frequently employed in the synthesis of various heterocyclic compounds.

How is Methyl-D3-Amine Hydrochloride typically used in organic synthesis?

MDAH is typically used as a solution in a suitable solvent such as methanol or ethanol. It is added to the reaction mixture in specific amounts based on the desired stoichiometry. MDAH can be used in conjunction with other reagents to facilitate various types of reactions. The reaction mixture is typically heated and stirred to promote the reaction between MDAH and the targeted compound. Once the reaction is complete, MDAH is usually removed through extraction or evaporation processes.

What are the advantages of using Methyl-D3-Amine Hydrochloride in organic synthesis?

One of the main advantages of using MDAH in organic synthesis is its high reactivity as a nucleophile. This allows for efficient and selective bond formation in a variety of chemical reactions. MDAH is also relatively cost-effective compared to other reagents with similar reactivity. Additionally, MDAH is stable under typical storage conditions, making it easy to handle and store. Its versatility in different types of reactions and its compatibility with various functional groups make MDAH a valuable tool in organic synthesis.

Are there any safety considerations when working with Methyl-D3-Amine Hydrochloride?

As with any chemical reagent, it is important to handle MDAH with caution. It is recommended to use appropriate personal protective equipment such as gloves, goggles, and a lab coat when working with MDAH. Since MDAH is a strong nucleophile, it should be handled in a well-ventilated area to prevent exposure to potentially harmful vapors. It is also important to carefully follow the recommended procedures for storage, handling, and disposal of MDAH to ensure safety in the laboratory.
Leave A Message
Leave A Message ×
If you are interested in our products and want to know more details,please leave a message here,we will reply you as soon as we can.